Evidence map›Paper›PMID 21146469›Full record

Trial reportThe journal of pain2011

Drug response profiles to experimental pain are opioid and pain modality specific.

Lindsay L Kindler, Kimberly T Sibille, Toni L Glover, Roland Staud, Joseph L Riley, Roger B Fillingim

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in The journal of pain, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 23 citations in OpenAlex.

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  10. Peripheral Mechanisms of Ischemic Myalgia.Frontiers in cellular neuroscience · 2017
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Lindsay L KindlerComprehensive Center for Pain Research, University of Florida College of Dentistry, Gainesville, Florida, USA.
Kimberly T Sibille
Toni L Glover
Roland Staud
Joseph L Riley
Roger B Fillingim
Florida College · USUniversity of Florida · US

Funding

Risk Factors for Onset and Persistence of TMDU01DE017018 · NIDCR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DIATCHENKO, LUDA, FILLINGIM, ROGER B · 2005 to 2016
$35.9M
University of Florida Older Americans Independence Center (OAIC)P30AG028740 · NIA · UNIVERSITY OF FLORIDA · PI CHRISTIAAN LEEUWENBURGH · 2007 to 2026
$22.8M
UF CLINICAL AND TRANSLATIONAL SCIENCE AWARDUL1RR029890 · NCRR · UNIVERSITY OF FLORIDA · PI NELSON, DAVID R · 2009 to 2011
$14.4M
Sex-Related Genetic Influences on Pain and AnalgesiaR01NS041670 · NINDS · UNIVERSITY OF FLORIDA · PI FILLINGIM, ROGER B · 2000 to 2009
$4.4M
Integrative and translational training in pain researchT32NS045551 · NINDS · UNIVERSITY OF FLORIDA · PI YEZIERSKI, ROBERT P. · 2005 to 2014
$1.8M
NCRR NIH HHS RR029890NCRR NIH HHS UL1 RR029890NIA NIH HHS P30 AG028740NIDCR NIH HHS U01 DE017018NINDS NIH HHS NS045551NINDS NIH HHS R01 NS041670NINDS NIH HHS T32 NS045551
6 · The paper itself

Abstract

unlabelledGiven our limited ability to predict analgesic efficacy, further research is needed to understand factors influencing analgesic response patterns. The aim of this study was to better understand the relationship between morphine and butorphanol analgesic efficacy tested against multiple pain modalities within the same individuals. Participants included healthy men (n = 72) and women (n = 67) who underwent thermal, pressure, and ischemic experimental pain testing before and after the double-blind administration of morphine and butorphanol during separate testing sessions. Factor analysis revealed 6 factors with analgesic effects grouped primarily by pain modality and specific to either morphine or butorphanol. Hierarchical cluster analysis of individual factor scores led to 4 distinct drug response profiles. Three groups displayed exceptional analgesic efficacy produced by 1 type of opioid on 1 pain stimulus modality, whereas the fourth drug response profile was characterized by average analgesic efficacy across all pain modalities for both opioids. These findings suggest that opioids with varying efficacy at the μ and κ receptors produce independent effects on unique pain mechanisms and that individual responsiveness for some is dependent on pain mechanism and opioid type, although a subset of the population is moderately responsive to opioids regardless of efficacy of receptor binding or predominant pain mechanism being activated. PERSPECTIVE: This investigation provides a foundation for understanding patterns of opioid efficacy in varying types of pain. Our findings suggest that opioid response patterns are more complex than originally thought with about half of individuals exhibiting opioid and pain modality specific analgesic response profiles.

Indexed as

AdolescentAdultAnalgesics, OpioidButorphanolCluster AnalysisDouble-Blind MethodFemaleHumansMaleMiddle AgedMorphinePainPain MeasurementPain ThresholdPressurePsychological TestsAnalgesics, OpioidButorphanolMorphineReceptors, Opioid, kappaReceptors, Opioid, mu

Identifiers

PMID21146469
PMCPMC3052955
OpenAlexW2089517184

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.